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Function and structure of peculiar yeast alcohol dehydrogenases of which activities are reversibly inhibited by Zn^<2+>

Research Project

Project/Area Number 04660101
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field 応用微生物学・発酵学
Research InstitutionChiba University

Principal Investigator

FUJII Takaki  Chiba Univ.Bioproduction Science professor, 園芸学部, 教授 (50125952)

Co-Investigator(Kenkyū-buntansha) SHINOYAMA Hirofumi  Chiba Univ.Bioproduction Science assistant professor, 園芸学部, 助教授 (40211958)
安藤 昭一  千葉大学, 園芸学部, 教教授 (80125898)
Project Period (FY) 1992 – 1993
Project Status Completed (Fiscal Year 1993)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1993: ¥300,000 (Direct Cost: ¥300,000)
Fiscal Year 1992: ¥1,700,000 (Direct Cost: ¥1,700,000)
KeywordsAlcohol dehydrogenase / methanol-utilizing yeast / zinc ion-inhibition / candida sp. / アイソザイム / 亜鉛イオン / エタノール資化 / ホルムアルデヒド / アセトアルデヒド
Research Abstract

We found that a methanol utilizing yeast, Candida sp. N-16, had two types of NAD-dependent alcohol dehydrogenases. One was a constitutive enzyme (ADH-MI) and the other and inducible enzyme (ADH-MII). These enzyme were inhibited by Zn^<2+>.
The purified preparation of ADH-MII was examined in the presence of Zn^<2+> by circular dichroism (CD) analyze. The CD spectrum of ADH-MII was different from those of ADHs from horse liver and baker's yeast. These spectral data indicate that the conformation of ADH-MII changed in the presence of Zn^<2+>. Besides, 20 N-terminal amino acids of ADH-MII were determined.
ADH-MI was extremely unstable, but remained stable in the presence of ammonium sulfate (about 800 mM). The enzyme was purified in the presence of ammonium sulfateas an electrophoretically homogeneous protein from cells grown on ethanol. The molecular weight of the native enzyme was estimated to be about 120,000. It consisted of two subunits (90,000 and 40,000). The Km values for ethanol and NAD were 1.25 x 10^<-3> M and 6.25 x 10^<-5> M, respectively. The Ki value for Zn^<2+> was 5.35 x 10^<-5> M.
Alcohol dehydrogenase activities in cell-free extracts prepared from other methanol-utilizing yeasts, Hansenula polymorpha and Pichia pastoris, were also inhibited by a low concentration of Zn^<2+>.

Report

(3 results)
  • 1993 Annual Research Report   Final Research Report Summary
  • 1992 Annual Research Report
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] 藤井貴明: "酸化性酵母のアルコール脱水素酵素:メタノール資化性酵母に存在するZn^<2+>で阻害される酵素" 日本生物工学会誌. 71. 270 (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] Takaaki Fujii: "Alcohol dehydrogenases in oxidative yeasts : Peculiar enzymes inhibited by Zn^<2+> in a methanol-utilizing yeast." Seibutsukougaku. 71. 270 (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1993 Final Research Report Summary
  • [Publications] 藤井貴明: "酸化性酵母のアルコール脱水素酵素:メタノール資化性酵母に存在するZn^<2+>で阻害される特異な酵素" 日本生物工学会誌. 71. 270 (1993)

    • Related Report
      1993 Annual Research Report

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Published: 1992-04-01   Modified: 2016-04-21  

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